Depth of response prior to autologous stem cell transplantation predicts survival in light chain amyloidosis.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
04 2021
Historique:
received: 28 04 2020
accepted: 03 11 2020
revised: 25 08 2020
pubmed: 20 11 2020
medline: 9 7 2021
entrez: 19 11 2020
Statut: ppublish

Résumé

The goal of therapy in AL amyloidosis is to inhibit further production of the amyloidogenic light chains, thereby allowing organ recovery and improving survival. We aimed to assess the impact of depth of hematologic response prior to ASCT on survival. We conducted a retrospective study of 128 newly diagnosed AL amyloidosis patients who received induction prior to ASCT between January 2007 and August 2017 at Mayo Clinic. The overall response rate to induction was 86% (CR 18%, VGPR 31% and PR 38%). With a median follow up of 52 months, the median PFS and OS was 48.5 months and not reached, respectively. Response depth to induction therapy was associated with improved PFS and OS. The median PFS was not reached for patients achieving ≥VGPR prior to ASCT and 34.1 months for patients achieving PR or less (P = 0.0009). The median OS was longer in patients with deeper responses (not reached for ≥VGPR vs. 128 months for PR or less (P = 0.02)). On multivariable analysis, independent predictors of OS were melphalan conditioning dose (RR = 0.42; P = 0.036) and depth of response prior to transplant (RR 0.37; P = 0.0295). Hematologic response prior to transplant predicts improved post transplant outcomes in AL amyloidosis.

Identifiants

pubmed: 33208916
doi: 10.1038/s41409-020-01136-2
pii: 10.1038/s41409-020-01136-2
doi:

Substances chimiques

Melphalan Q41OR9510P

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

928-935

Subventions

Organisme : NCI NIH HHS
ID : P50 CA186781
Pays : United States

Commentaires et corrections

Type : CommentIn

Références

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Auteurs

Iuliana Vaxman (I)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Institute of Hematology, Davidoff Cancer Center, Rabin Medical Center, Petah-Tikva, Israel.
Israel Sackler Faculty of Medicine Tel-Aviv University, Tel-Aviv, Israel.

M Hasib Sidiqi (MH)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.
Fiona Stanley Hospital, Perth, WA, Australia.

Abdullah S Al Saleh (AS)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.
King Saud bin Abdulaziz University for Health Sciences, Riyadh, Saudi Arabia.

Shaji Kumar (S)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Eli Muchtar (E)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Angela Dispenzieri (A)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Francis Buadi (F)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

David Dingli (D)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Martha Lacy (M)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Suzanne Hayman (S)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Nelson Leung (N)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Wilson Gonsalves (W)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Taxiarchis Kourelis (T)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Rahma Warsame (R)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

William Hogan (W)

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Morie Gertz (M)

Division of Hematology, Mayo Clinic, Rochester, MN, USA. gertz.morie@mayo.edu.

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